Xiang Tong, Wang Qiao, He Biwen, Zhang Jibo, Huang Xixi, Chen Wei, Luo Siwei, Qi Xiang
Hunan Key Laboratory for Micro-Nano Energy Materials and Devices, School of Physics and Optoelectronics, Xiangtan University, Hunan 411105, China.
Department of Physics, School of Science, Institute of Quantum Science and Technology, Shanghai University, Shanghai 200444, China.
J Phys Chem Lett. 2025 Jun 19;16(24):6212-6218. doi: 10.1021/acs.jpclett.5c01197. Epub 2025 Jun 12.
Surface-enhanced Raman scattering (SERS) technology is highly sensitive but limited by the high cost of noble-metal substrates and the low enhancement of two-dimensional (2D) materials. This work proposes a dual-sided adsorption strategy utilizing warped structures at the cracks and edges of WSe and MoSe nanosheets grown by Chemical Vapor Deposition (CVD). Driven by capillary forces, probe molecules infiltrate the nanosheet-substrate interface, enabling dual-sided adsorption on both the upper and lower surfaces. This approach enhances SERS signals by up to 20-fold, with a detection limit of 10 M, surpassing most reported traditional single-sided adsorption modes. Additionally, it improves stability by isolating the probe molecules from oxygen. This study further enhanced the formation efficiency and coverage area of the dual-sided adsorption mode by leveraging wide warped structures. It offers new perspectives on the application of crack defects and the potential for the development of high-performance and highly stable SERS substrates.
表面增强拉曼散射(SERS)技术灵敏度高,但受限于贵金属基底的高成本以及二维(2D)材料增强效果低的问题。本研究提出一种双面吸附策略,利用化学气相沉积(CVD)生长的WSe和MoSe纳米片裂缝及边缘处的翘曲结构。在毛细作用力驱动下,探针分子渗透到纳米片-基底界面,实现上下表面的双面吸附。该方法将SERS信号增强高达20倍,检测限达10 M,超过大多数已报道的传统单面吸附模式。此外,通过将探针分子与氧气隔离提高了稳定性。本研究通过利用宽翘曲结构进一步提高了双面吸附模式的形成效率和覆盖面积。它为裂纹缺陷的应用以及高性能、高稳定性SERS基底的开发潜力提供了新视角。